Giacomina Rossi

Fondazione IRCCS Istituto Neurologico "C. Besta"

Emailgiacomina.rossi@istituto-besta.it

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103 Article
2 Letter

Disease-related cortical thinning in presymptomatic granulin mutation carriers
Genetic FTD Initiative (GENFI), Jan 2021, In: NeuroImage: Clinical. 29, 102540.
Research output: Contribution to journal › Article › peer-review

Open Access
Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes
International FTD-Genomics Consortium, 2021, (Accepted/In press) In: Biological Psychiatry.
Research output: Contribution to journal › Article › peer-review
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia
the EU EOD Consortium & IFGC, 2021, In: Neurobiology of Aging. 99, p. 99.e15-99.e22
Research output: Contribution to journal › Article › peer-review
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
The American Genome Center (TAGC), The FALS Sequencing Consortium, The Genomics England Research Consortium, The International ALS/FTD Genomics Consortium (iAFGC), The International FTD Genetics Consortium (IFGC), The International LBD Genomics Consortium (iLBDGC), The NYGC ALS Consortium, the University of Maryland Brain and Tissue Bank and NIH NeuroBioBank & The PROSPECT Consortium, Feb 3 2021, In: Neuron. 109, 3, p. 448-460.e4
Research output: Contribution to journal › Article › peer-review
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts
International FTD-Genetics Consortium, Costa, B., Manzoni, C., Bernal-Quiros, M., Kia, D. A., Aguilar, M., Alvarez, I., Alvarez, V., Andreassen, O., Anfossi, M., Bagnoli, S., Benussi, L., Bernardi, L., Binetti, G., Blackburn, D., Boada, M., Borroni, B., Bowns, L., Bråthen, G., Bruni, A. C. & 32 others, Chiang, H. H., Clarimon, J., Colville, S., Conidi, M. E., Cope, T. E., Cruchaga, C., Cupidi, C., Di Battista, M. E., Diehl-Schmid, J., Diez-Fairen, M., Dols-Icardo, O., Durante, E., Flisar, D., Frangipane, F., Galimberti, D., Gallo, M., Gallucci, M., Ghidoni, R., Graff, C., Grafman, J. H., Grossman, M., Hardy, J., Hernández, I., Holloway, G. J. T., Novelli, V., Puca, A. A., Rossi, G., Scarpini, E., Serpente, M., Nacmias, B., Sorbi, S. & Tagliavini, F., Dec 15 2020, In: Neurology. 95, 24, p. e3288-e3302
Research output: Contribution to journal › Article › peer-review

Open Access

Disease-related cortical thinning in presymptomatic granulin mutation carriers

Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts